BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1934587 · Received December 4, 2010

    Report

    Report Number
    1831750-2010-04424
    Event Type
    Malfunction
    Date Received
    December 4, 2010
    Date of Event
    September 20, 2010
    Report Date
    September 20, 2010
    Manufacturer
    STRYKER CORP, MED DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION: REPLACEMENT FOOT COVER ASSEMBLIES ARE BEING SENT TO THE HOSP.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT COVER ASSEMBLY WAS GETTING CAUGHT ON THE LIFT MOTOR HEADER. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP, MED DIV. 3002S3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1